NCT07599709CompletedNot Applicable
LONG PULSED ND:YAG LASER (1064 NM) VERSUS INTENSE PULSED LIGHT IN TREATMENT OF TRAUMATIC AND POST-SURGICAL ERYTHEMATOUS SCARS
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Alexandria University
- Enrollment
- 40
- Locations
- 1
Study Overview
Brief Summary
The goal of this clinical trial is to compare the efficacy and safety of long-pulsed ND:YAG laser and intense pulsed light in the treatment of traumatic and post-surgical erythematous scars. Forty patients presenting with traumatic and post-surgical erythematous scars on the head and neck, of six months' duration or less, were randomly divided into two equal groups. Group A patients received long-pulsed ND:YAG laser sessions, while Group B patients received intense pulsed light sessions. Four sessions were given at four-week intervals.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Eligibility Criteria
- Ages
- 12 Years to — (Child, Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients of either gender, aged more than 12 years, presenting with an erythematous scar on the head and neck area, traumatic or post-surgical, and of a duration equal to or less than six months.
Exclusion Criteria
- •1. Patients with post burn scars, scars of more than six months duration, keloids, post acne atrophic erythematous scars or scars that are not located on the head and neck area.
- •2. Patients with active bacterial, viral, or fungal cutaneous infection within the scar tissue.
- •3. Patients who are pregnant or lactating.
- •Known contraindication to laser therapy.
- •Use of Isotretinoin within the previous 6 months.
Investigators
Study Sites (1)
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